Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685652Generated: October 29, 2026

N-bromobutanimide → 3-Benzoyloxy-4-chlorobenzyl bromide

https://huagongshe.com/reaction/1685652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Benzoyloxy-4-fluorobenzyl bromideHCID 16747838—
Reactant3-Benzoyloxy-4-chlorotolueneHCID 16749222—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product3-Benzoyloxy-4-chlorobenzyl bromideHCID 1674784062%

Reaction Steps

The title compound was prepared by adapting the method for 3-benzoyloxy-4-fluorobenzyl bromide using 3-benzoyloxy-4-chlorotoluene (2.47 g, 10.0 mmol), NBS (1.96 g, 11.0 mmol) and benzoyl peroxide (10 mg) in carbon tetrachloride (25 mL). The residue was purified by flash column chromatography [SiO2, EtOAc/n-hexane (1:40)] to give 3-benzoyloxy-4-chlorobenzyl bromide as a colourless oil (2.012 g, 62%) which solidified on standing and was used without further purification; δH (400 MHz, CDCl3) 4.48 (s, 2H), 7.27 (dd, J=8.2, 2.0, 1H), 7.36 (d, J=2.0, 1H), 7.46 (d, J=8.2, 1H), 7.50-7.58 (m, 2H), 7.64-7.71 (m, 1H), 8.22-8.28 (m, 2H). LRMS (FAB+) m/z (rel. intensity) 325.0 (81, [M+H]+), 327.0 (100, [M+H]+);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148415B2
Source datasetuspto-grants-2012_04
ORD IDord-78b5aac6856f4760a1c64fee63a8c8f6
Source noteuspto-grants-2012_04